Canonical Allele Identifier: CA340730136

Gene: IL23R

Linked Data

• MyVariant Identifiers: chr1:g.67724798T>C (hg19) ; chr1:g.67259115T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67259115T>C , CM000663.2:g.67259115T>C	GRCh38
NC_000001.10:g.67724798T>C , CM000663.1:g.67724798T>C	GRCh37
NC_000001.9:g.67497386T>C	NCBI36
NG_011498.1:g.97630T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000697149.1:c.1716T>C	ENSP00000513138.1:n.1716T>C
ENST00000697150.1:c.1774T>C	ENSP00000513139.1:n.1774T>C
ENST00000697151.1:c.1707T>C	ENSP00000513140.1:n.1707T>C
ENST00000697164.1:c.1787T>C	ENSP00000513153.1:p.Leu596Pro
ENST00000697165.1:c.1574T>C	ENSP00000513154.1:p.Leu525Pro
ENST00000347310.10:c.1877T>C MANE Select	ENSP00000321345.5:p.Leu626Pro
ENST00000637002.1:c.1268T>C	ENSP00000490340.1:p.Leu423Pro
ENST00000347310.9:c.1877T>C	ENSP00000321345.5:p.Leu626Pro
ENST00000395227.2:c.671T>C	ENSP00000378652.2:p.Leu224Pro
ENST00000425614.3:c.1112T>C	ENSP00000387640.2:p.Leu371Pro
ENST00000473881.2:c.*703T>C	ENSP00000486667.1:n.*703T>C
NM_144701.2:c.1877T>C	NP_653302.2:p.Leu626Pro
XM_005270516.2:c.1115T>C	XP_005270573.1:p.Leu372Pro
XM_011540789.1:c.1967T>C	XP_011539091.1:p.Leu656Pro
XM_011540790.1:c.1877T>C	XP_011539092.1:p.Leu626Pro
XM_011540791.1:c.1877T>C	XP_011539093.1:p.Leu626Pro
XM_011540790.3:c.1877T>C	XP_011539092.1:p.Leu626Pro
XM_011540791.3:c.1877T>C	XP_011539093.1:p.Leu626Pro
XR_001736993.1:n.1957T>C
NM_144701.3:c.1877T>C MANE Select	NP_653302.2:p.Leu626Pro